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rs10877839

From SNPedia

Orientationplus
Stabilizedplus
Make rs10877839(C;C)
Make rs10877839(C;T)
Make rs10877839(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position62424701
is asnp
is mentioned by
dbSNPrs10877839
dbSNP (classic)rs10877839
ClinGenrs10877839
ebirs10877839
HLIrs10877839
Exacrs10877839
Gnomadrs10877839
Varsomers10877839
LitVarrs10877839
Maprs10877839
PheGenIrs10877839
Biobankrs10877839
1000 genomesrs10877839
hgdprs10877839
ensemblrs10877839
geneviewrs10877839
scholarrs10877839
googlers10877839
pharmgkbrs10877839
gwascentralrs10877839
openSNPrs10877839
23andMers10877839
SNPshotrs10877839
SNPdbers10877839
MSV3drs10877839
GWAS Ctlgrs10877839
GMAF0.3021
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23382691OA-icon.png]
Trait IgG glycosylation
Title Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Risk Allele C
P-val 9E-6
Odds Ratio .15 [0.082-0.21] unit decrease